eudamed_udi
Primary ID: 07040670282644
Unspecified Brand (UDI 07040670282644)
Manufactured by Glamox AS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 07040670282644
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: LHH G2 T105 AWh 900 935-945 CCT TR CLA EU ( Only for OKB Med) is a medical device manufactured by Glamox AS. This product is indexed under FDA Product Code / Category Classification Z120499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LHH G2 T105 AWh 900 935-945 CCT TR CLA EU ( Only for OKB Med
- Product Code / EMDN
- Z120499
- Device Name
- LHH G2
- Database Sync Date
- 2026-08-09 16:46:54
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Glamox AS.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07040670282644.
What classification code is assigned to this device?
This device is registered under product classification code Z120499.
Similar Classification Devices (Z120499)
Other Devices by Glamox AS
Programmatic Export
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JSON API Endpoint